Canonical Allele Identifier: CA393585997

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78894479C>A (hg19) ; chr15:g.78602137C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602137C>A , CM000677.2:g.78602137C>A	GRCh38
NC_000015.9:g.78894479C>A , CM000677.1:g.78894479C>A	GRCh37
NC_000015.8:g.76681534C>A	NCBI36
NG_016143.1:g.24159G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.505G>T MANE Select	ENSP00000315602.5:p.Asp169Tyr
ENST00000326828.5:c.505G>T	ENSP00000315602.5:p.Asp169Tyr
ENST00000348639.7:c.505G>T	ENSP00000267951.4:p.Asp169Tyr
ENST00000558903.1:n.212G>T
ENST00000559658.5:c.505G>T	ENSP00000452896.1:p.Asp169Tyr
NM_000743.4:c.505G>T	NP_000734.2:p.Asp169Tyr
NM_001166694.1:c.505G>T	NP_001160166.1:p.Asp169Tyr
NR_046313.1:n.1006G>T
XM_006720382.1:c.304G>T	XP_006720445.1:p.Asp102Tyr
XM_011521173.1:c.424G>T	XP_011519475.1:p.Asp142Tyr
XM_006720382.3:c.304G>T	XP_006720445.1:p.Asp102Tyr
NM_000743.5:c.505G>T MANE Select	NP_000734.2:p.Asp169Tyr
NM_001166694.2:c.505G>T	NP_001160166.1:p.Asp169Tyr
NR_046313.2:n.707G>T